proline and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis

proline has been researched along with Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baraitser, M; Malcolm, S; Rutland, P; Strautnieks, S; Winter, RM	1

Other Studies

1 other study(ies) available for proline and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis

Article	Year
Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosis. American journal of human genetics, 1992, Volume: 51, Issue:4 Topics: Amino Acid Sequence; Base Sequence; Chorionic Villi Sampling; Diffuse Cerebral Sclerosis of Schilder; DNA; Exons; Female; Genetic Counseling; Humans; Infant, Newborn; Leucine; Male; Molecular Sequence Data; Myelin Proteins; Myelin Proteolipid Protein; Oligodeoxyribonucleotides; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Pregnancy; Prenatal Diagnosis; Proline; Restriction Mapping; Threonine; X Chromosome	1992

Article

Year

Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosis.

American journal of human genetics, 1992, Volume: 51, Issue:4

Topics: Amino Acid Sequence; Base Sequence; Chorionic Villi Sampling; Diffuse Cerebral Sclerosis of Schilder; DNA; Exons; Female; Genetic Counseling; Humans; Infant, Newborn; Leucine; Male; Molecular Sequence Data; Myelin Proteins; Myelin Proteolipid Protein; Oligodeoxyribonucleotides; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Pregnancy; Prenatal Diagnosis; Proline; Restriction Mapping; Threonine; X Chromosome

1992